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Pharma Job : Manager Openings @ Zydus Cadila

Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. The group has state-of-the-art vertically integrated manufacturing facilities for APIs and Formulations, spread across five states of Gujarat, Maharashtra, Goa, Himachal Pradesh and Sikkim.

Job Title – Dy. Manager – Manufacturing Excellence and Investigator

No.of.Openings – 2

Experience – 5 – 10 Years

Location – Panjim/Panaji

Job Description:

A. Manufacturing Excellence (1 Position) :

  • Responsible for manufacturing excellence initiatives at plant level.
  • Responsible for taking initiatives in improvement of all aspects of working processes and methodologies.
  • Predictive analytics improvement of operational parameters like Yield, cycle time, equipment efficiency, Process Cycle Efficiency, CPP trending etc.
  • Leading the OEE (Overall Equipment Efficiency) program for the formulation plants to diagnose and identify opportunities to improve OEE.
  • Architect for Lean Six Sigma framework.
  • Having experience in Process capability Improvement, DMAIC/8D methodology, Statistical analysis and other Operational Excellence tools. Should be acquainted with application like Minitab , Visio and Quality Companion.
  • Must have worked in regulated plants having approvals of US FDA, MHRA. etc.
  • Hands-on experience in handling and implementing cGMP (Current Good Manufacturing Practice) practices and Good Documentation Practices.
  • Technically competent on all aspects of Tablet /capsule manufacturing with FDA approval.

B. Investigator/Trouble shooting (1 Position)

  • Relevant experience of IPQA Activities / QMS/
  • Assessment of change controls relating to risk management and gap analysis.
  • Preparation and review of Failure Investigation Reports against Quality Impacting deviations, Out-of-Specifications and major Non-Conformances.
  • Market Complaints and Regulatory Audit observations / Identification of scope for implementation of Preventive Action to mitigate or reduce risk of recurrence in oral solid dosage/ Injectable Manufacturing facilities.
  • Must have worked in regulated plants having approvals of US FDA, MHRA. etc.
  • Hands-on experience in handling and implementing cGMP (Current Good Manufacturing Practice) practices and Good Documentation Practices.
See Also  Project Assistant Position for Chemistry Candidates @ Rajiv Gandhi University

 

Desired Profile:

  • UG – B.Pharma – Pharmacy 
  • PG – M.Pharma – Pharmacy

Click here to Apply Online

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